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    NDC 69848-0012-25 Ibuprofen 200 mg/1 Details

    Ibuprofen 200 mg/1

    Ibuprofen is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Granules USA, Inc.. The primary component is IBUPROFEN.

    Product Information

    NDC 69848-0012
    Product ID 69848-012_0d1d24e9-1861-af97-e063-6394a90a6e29
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Ibuprofen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name Granules USA, Inc.
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA079174
    Listing Certified Through 2024-12-31

    Package

    NDC 69848-0012-25 (69848001225)

    NDC Package Code 69848-012-25
    Billing NDC 69848001225
    Package 250 TABLET in 1 BOTTLE (69848-012-25)
    Marketing Start Date 2019-07-01
    NDC Exclude Flag N
    Pricing Information N/A